Gadolinium oxide host and europium/dysprosium/terbium doped gadolinium oxide nanoparticles were synthesized using the sonochemical technique. Gadolinium oxide nanocrystals were also co-doped with total 2 mol% of Eu(3+)/Dy(3+),Eu(3+)/Tb(3+),Dy(3+)/Tb(3+), and also Eu(3+)/Dy(3+)/Tb(3+) ions, by the same method. The nanoparticles obtained were characterized using powder x-ray diffraction (XRD), transmission electron microscopy (TEM), and selected area electron diffraction (SAED) techniques. The size of the particles ranged from 15 to 30 nm. The triple doped samples showed multicolor emission on single wavelength excitation. The photoluminescence results were correlated with the lifetime data to get an insight into the luminescence and energy transfer processes taking place in the system. On excitation at 247 nm, the novel nanocrystalline Gd(2)O(3):RE (RE = Dy, Tb) phosphor resulted in having very impressive CIE chromaticity coordinates of x = 0.315 and y = 0.316, and a correlated color temperature of 6508 K, which is very close to standard daylight.

Nanocrystalline YCrO3 powder was synthesized by a combustion technique using glycine as the fuel and the corresponding metal nitrates as oxidants. Three different oxidant-to-fuel ratios namely fuel-deficient, stoichiometric and fuel-excess ratios were chosen to explore the possibility to prepare single-phasic YCrO3. The crystallite size for the phase pure product after calcination at 600 °C was found to be 36 nm by x-ray line broadening. The agglomerate behaviour was investigated by light scattering studies. The TEM observations clearly highlight the pronounced crystallinity for YCrO3. A striking observation was the presence of onion-like layers in HR-TEM micrographs. Magnetic measurements reveal the weak ferromagnetic nature of YCrO3 nanoparticles, although the bulk YCrO3 is reported to be an antiferromagnetic material.

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Highly sinter-active powders of RE2O3 [rare earth (RE) = Gd, Eu, Dy] have been prepared using the corresponding metal nitrates as the oxidants, and glycine and citric acid as the fuels. Two different oxidant-to-fuel ratios, namely stoichiometric ratio and fuel-deficient ratio were used to explore the possibility of preparing different crystallographic modifications. By a careful control of oxidant-to-fuel ratio, nanocrystalline Eu2O3 and Gd2O3 could be prepared in cubic (C-type) as well as monoclinic (B-type) modifications. However, the high-temperature monoclinic modification could not be obtained for Dy2O3 due to a very high C-to-B-type phase transition temperature. The crystallite size, surface area, and sintering behavior were also studied for powders prepared using different oxidant-to-fuel ratios, and the results showed a remarkable correlation between different fuel contents and powder properties. Some of these powders resulted in pellets of nearly theoretical density. The sintered microstructure was studied by scanning electron microscopy.

Twenty mol% gadolinium doped ceria powders were prepared by citrate-nitrate combustion synthesis technique. Two different sources of cerium viz. cerium nitrate and ammonium ceric nitrate were used in different oxidant-to-fuel ratios. The crystallite size of the synthesized powders ranged 5-27 nm was obtained depending on the preparation conditions with average particle size in the range 0.64-1.26 microm. Although, the powders were found to be agglomerated in nature, these powders were highly sinter-active as they showed very high sintered density (> or = 95%) when sintered at 1250 degrees C having grain size in the range of 200-500 nm. The electrical conductivity was found to depend on the temperature with two distinct regimes at a transition point of 350 degrees C. The grain boundary showed a significant role in the total conductivity with its activation energy dependent on the material preparation conditions. The activation energy of total conduction was found to be significantly low (-0.5 eV) in the temperature range of 400-700 degrees C, this property is unique for application as an electrolyte for solid oxide fuel cell operating in the low temperature range. It was found that a fuel-deficient combustion reaction using cerium nitrate as the oxidant yielded the best quality powder which showed a maximum electrical conductivity of -1.74 x 10(-2) S/cm at 600 degrees C.

Water dispersible Gd2O3:Dy3+ (2%) nanophosphors were synthesized through a facile polyol process and characterized by using X-ray diffraction (XRD), transmission electron microscopy (TEM), Dynamic Light Scattering (DLS) and photoluminescence (PL) spectrophotometry. The results of XRD, TEM and DLS show that resultant nanoparticles are single phasic and have spherical shape with 17 to 22% dispersibility. An efficient energy transfer was observed from host to the dopant ions. Characteristic blue and yellow emissions from Dy3+ ions were observed. The CIE coordinates of the nanophosphor lie in the white light region of the chromaticity diagram. Spin coating of the nanophosphor was done on quartz substrate. Bright white luminescence of this film was observed under ultraviolet light with lamda exc = 310 nm.

Smoothing of the fractal rough surface of Nd2O3 doped CeO2 ceramic under sintering has been observed in an ultra-small angle x-ray scattering investigation. The surface fractal dimension of 2.6 for the non-sintered specimen reduces with sintering temperature and gradually attains a value of 2.0, which corresponds to a smooth surface, at a high enough sintering temperature. A Monte Carlo based computer simulation has been attempted to explain the smoothing of such a fractally rough surface due to the diffusion based surface transport of the materials from a region of positive curvature to one of negative curvature. The variation of the interface width and the evolution of the fractal dimension with sintering have been estimated from this model simulation.